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Regulatory Documents Explained - DHF, DMR, DHR and TF
Автор: GlobalCompliance Panel
Загружено: 2016-07-13
Просмотров: 6089
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The FDA QSR and the Medical Device Directive specify certain records that should be included in your organization's quality system - Design History File (DHF), Device Master Record (DMR), Device History Record (DHR), and Technical File (TF).
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